Clinical Investigation to Assess the Safety and Feasibility of the Crestal, Minimal-invasive Sinus Floor Augmentation With the Pressure Chamber Drill (DKK) and the Sinus Vibration Pump (SVP)
NCT ID: NCT01204424
Last Updated: 2010-09-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE1
20 participants
INTERVENTIONAL
2010-09-30
2011-06-30
Brief Summary
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The conventional procedure for a sinus lift (Caldwell-Luc procedure) requires preparation of a mucoperiosteal flap in the buccal molar region and to cut an oval window in the thus exposed bone, without damage to the subjacent maxillary sinus membrane. The procedure is very invasive and subjects the patient to great stress as a result of substantial swelling and discoloration of up to 10 days, and possibly of pain. This surgical procedure is oftentimes referred to as "open" or "classic" sinus lift. This technique is fraught with many risks and complications because of the limitations of healing potential in the maxillary sinus. In spite of these risks many patients undergo this procedure because of the strong desire to replace missing maxillary teeth with dental implants.
An alternative approach to the maxillary sinus from the inferior approach of the alveolar ridge utilizing solid cylindrical osteotomes was described by Dr. Summers (crestal sinus lift). It is a more conservative approach and is less invasive. It was developed to eliminate the risks described above.While this technique is safer, an overzealous use of an osteotome during the placement of the regenerative material can result in the perforation of the subantral membrane with disadvantages discussed above.
Dr. Eder has developed an innovative way - the JEDER System - of carrying out a crestal sinus lift that substantially reduces the risk of perforating the subantral membrane. This minimal- invasive way uses 2 newly developed and successfully patented instruments, the "Druckkammerknochenfräse" DKK and the "Sinusvibrationspumpe" SVP. Following JEDER Syst. the mucous membrane of the mouth is opened from the toothless part of the maxillary crest up to the bone and the bone is scraped by a cylindrical cutter in the shape of a tunnel up to slightly underneath the maxillary sinus membrane.
The aim of the study is to assess the efficacy and safety of the JEDER Syst., which was already demonstrated in 50 treatment attempts. The results of this study will be used for the certification process to enable the declaration of conformity for the market approval.
The main outcome parameter is the perforation rate of the subantral membrane intraoperatively and within 6 weeks after the operation.
Risk benefit assessment:
In the present study there will be no additional examinations undertaken compared to patients which undergo the conventional procedure. The conventional procedure is associated with a risk of membrane perforation and consecutive diseases like infection, swelling and pain. All these inconveniences should be avoided by using the JEDER Syst. If the worst case scenario - the perforation of the subantral membrane - happens, the conventional method will be used. Therefore, the risk-benefit assessment
Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Interventions
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minimal-invasive sinus floor augmentation with the DKK and SVP (JEDER Syst.)
minimal-invasive sinus floor augmentation with the DKK and SVP (JEDER Syst.)
minimal invasive crestal sinus lift with the JEDER Systh.
The mucous membrane is opened from the toothless part of the maxillary crest up to the bone and the bone is scraped by a cylindrical cutter in the shape of a tunnel up to slightly underneath the maxillary sinus membrane and hydraulic pressure is being built up within the DKK. A centrally placed drill within the DKK slowly moves in the direction of the membrane. At the moment of the first minimal perforation of the remaining bone the pressurized fluid pushes the membrane back and ensures that the membrane is not perforated by the drill.
The SVP is used to generate hydraulic vibrations, which help to further raise the membrane from the bone (principle of the "percussion drill"). After the maxillary sinus membrane has successfully been elevated, the working fluid is extracted and bone replacement material is introduced via the bore.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* loss of teeth (regio 4 to 7)
* needed extraction of teeth (regio 4 to 7)
Exclusion Criteria
* severe chronic illness or immune deficiency
* cortisone therapy
* sinus membrane membrane hight \>5mm
* chronic sinusitis
* smoking \>20 Zigarettes
* missing dental hygiene
18 Years
90 Years
ALL
No
Sponsors
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Jeder GmbH
INDUSTRY
Responsible Party
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JEDER GmbH
Principal Investigators
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Michaela M Bayerle-Eder, Prof., MD, MBA
Role: STUDY_DIRECTOR
Medical University Vienna, Vienna Austria, Europe
Locations
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Ordination Dr. Klaus Eder
Vienna, Vienna, Austria
Countries
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Central Contacts
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Other Identifiers
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EK_10_101_0610
Identifier Type: OTHER
Identifier Source: secondary_id
DKK-SVP-10 Prot. 1.4
Identifier Type: -
Identifier Source: org_study_id